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3390/brainsci5010032
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brain sciences
ISSN 2076-3425
www.mdpi.com/journal/brainsci/
Review
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benefit from temporally and/or spatially associated multisensory information [16,27,28]. While
temporal synchrony refers to the capacity to specify whether a particular sound and image go together
or not, spatial synchrony concerns whether signals in diverse modalities comes from a common or
different location. The importance of synchrony for infant perception has been well documented [2931]
and is also reflected in the intermodal preference procedure, in which the bimodal information is
typically presented synchronously. It has been reported that on the basis of synchrony, newborn infants
are able to associate objects and linguistic stimuli [32] and that just a few hours old infants can learn
sight-sound pairings [31]. Bahrick (2001) [28] found that early as four weeks after birth, infants are
sensitive and able to learn arbitrary relations between audiovisual inputs, Moreover, it has been
demonstrated that infants between three and six months old have the ability to detect the difference and
discriminate temporal information of audio-visual inputs [33,34]. In addition, four-month-old infants
can connect and bind visual objects to the specific sounds produced by these objects [35,36]. For
instance, they are able to look longer at a puppet whose bouncing rate is the same as the rate at which
the sound occurred [35]. These signs of integration, detected early on in life, remind us that the
temporal synchrony is an important characteristic for MSI.
Behavioral benefits of early integration are imperative in the development of face and emotion
recognition and are important features in a childs abilities to adapt to his environment later in life.
Studies using a visual preference paradigm in a multimodal context for human faces have reported
interesting results in infants [3639]. For instance, two-month-old babies can link phonetic information
between voices and lip movements [39] and show an enhanced response when lip movements are
synchronized with sounds in contrast to unsynchronized ones [40]. In addition, four-month-old infants
can perceive affect (joy, sadness or anger) in words that are supported by audio-visual presentations [41],
and discriminate these affects in a multimodal context (i.e., establishing relations between faces (visual
modality) and voices (auditory modality) [41,42]. Overall, this data might support a form of
multisensory association present early on in life, favoring the innate hypothesis for MSI development.
However, all studies include post-natal investigations, which limits the opportunity to draw firm
conclusions. Studies on children born prematurely could be used to make more compelling arguments
in favor of this hypothesis and could be an interesting avenue of research. Also, evidence of
multisensory processes in newborns and infants has been demonstrated largely by behavioral data and
needs further investigation. Few researches have been carried to study the presence of multisensory
mechanisms using neuroimaging techniques. Ethical and practical limitations such as recruitment may
have diminished the possibility to undertake such studies on newborns. Nevertheless, the few studies
found in the literature will be discussed in Section 2.2.
2.1.2. The Late Integration Approach
In opposition to the Early Integration Approach, the Late Integration Approach emphasizes the
acquired nature of MSI. According to this hypothesis, all sensory systems work independently of each
other at birth. At this time, these systems are not mature and become increasingly refined during the
childs development. This is a long-term process during which cognitive changes and neuronal
reorganization keep going on until adolescence in which the brain must continuously adapt its neuronal
networks between sensory and motor communications [43]. In support of this, Putzar and colleagues
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(2007) [44] have recently shown that temporary visual deprivation in the first two years of life affects
the level of audio-visual integration that can be achieved once normal vision is restored. These
difficulties also persisted into adulthood [44]. This suggests that a critical period in infants
development might underlie the emergence and maturation of MSI, therefore reaching maturity
ontogenetically late. During the first months of life, contact with multisensory information seems to be
a prerequisite to develop and refine integration of these various sources of information. Thus, if
relevant experience is not gained in infancy, individuals cannot compensate for this loss later in life [45].
Furthermore, the various senses do not develop at the same rate. For instance, in humans, all the
sensory systems are functional at varying degrees by the end of gestation as these systems progress
towards full structural and functional maturity. Sensory structures underlying touch seem to be the first
to emerge during ontogenesis [46], followed by the onset of functional hearing (third trimester) and the
development of the visual system (largely after birth) [47,48]. While these findings indicate that there
is a difference in the rate at which the various sensory systems develop between one another, there is
also a difference in the way diverse characteristics develop within each of these systems. For instance,
visual acuity and contrast sensitivity keep improving until the child is five- or six-years-old [49], while the
period between two and five years of age is the time of development of perceptual language [50], which
corresponds to the processing of speech signal, both acoustically and visually. A study by
Morrongiello et al. (1994) [51] found an age effect in their study on object exploration and object
recognition in children between 3 and 8 years of age with common objects of different sizes. Their
results showed a distinct developmental pattern: Older children were faster, recognized more objects
and were more thorough in their exploratory strategies than the younger children [51]. Moreover, object
handling skills improve until the child is 8- to 14-year-old [52]. Thus, the child will have to learn to
integrate multisensory information during his development [13].
Recent studies conducted on very young infants have also suggested that post-natal experience
might contribute to MSI development [53]. Neil and colleagues (2006) [54] have studied the
development of eye and head movements in 1- to 10-month-old infants while they were subjected to
auditory, visual and audio-visual stimuli. Results showed that only 8- to 10-month-old infants
responded significantly faster in bimodal conditions than in unimodal conditions, suggesting that
audio-visual integration emerges at a late stage in the first year of life. Other studies have supported
the assumption that the integration of different modalities does not become optimal until relatively late
in childhood. In contrast to adults, when confronted to different sources of information from various
sensory modalities, children do not optimally integrate the information from the two sensory
modalities but make their perceptual judgments based only on one or the other sense. This unisensory
dominance has been found in visuo-tactile integration task [55], visual and tactile cues for size and
orientation discrimination [27], nonvisual self-motion and visual landmark information [56], in
judgments of surface slant based on stereoscopic and texture information [57] and in audio and visual
space and time perception [58]. According to Burr and Gorri (2011) [59], this unisensory dominance in
which the most robust modality is employed to tune the others could reflect a process of cross-sensory
calibration. As stated in the previous studies, MSI has not reached maturity in children younger than
eight years old [27,5558].
A number of authors have also put forward the presence of a MSI temporal window over which the
strength of multisensory interactions is dependent on the spatial and temporal synchrony between
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different sensory inputs [6062]. The more remote in space and time two sensory stimuli are, the less
likely they are to fuse. A behavioral study by Hillock and colleagues (2011) [63], reported that the
audio-visual integration temporal window is still immature in 10- and 11-year-old children, which
supports the hypothesis that the underlying plasticity and maturation of MSI continues
through development.
Unlike adults, behavioral studies have reported immature multisensory processing capacities in
children and adolescents in audio-visual discrimination tasks [6365] and in other sensory modalities [56].
For instance, Barutchu and colleagues [64,65] reported that multisensory facilitation is still immature
in 10-year-old children during a simple audio-visual detection task. In accordance with the Late
Integration Theory, results from these studies suggest that information acquired through various
sensory modalities might not be integrated optimally in very young infants and that optimal MSI only
occurs in children older than eight years [27,56] with changes occurring over a prolonged time course
that may extend into adolescence.
Animal studies have corroborated the notion that the brain is immature and must learn to combine
the various types of sensory information. One of the most studied neural structure in MSI is the cat
superior colliculus (SC), a midbrain structure in which neurons located in the deep layers are
responsible to converge multisensory inputs [66]. These multisensory neurons are responsible, among
other things, to detect and orient ones behavior to external events and sensory stimuli [6770]. Visual,
auditory and somatosensory inputs stimulate the SC and each sensory modality is represented in a
map-like representation in which all the different maps overlap each other and are in close topographic
register. Therefore, the alignment among the sensory maps is fundamental for multisensory neurons to
integrate the inputs from various senses manifesting itself into an adequately behavioral response [71].
Nevertheless, according to Wallace and colleagues (1997, 2006) [72,73] multisensory neurons found in
the SC are not present at the cortical and sub-cortical levels immediately after birth and it is only after
several months of life and exposure to a multisensory environment that the integration-specialized
neurons progressively appear and mature in the cat. Although the appearance of the first multisensory
neurons in kittens is at about ten days of age, their ability to integrate inputs from multiple sensory
modalities that can be considered adult-like is not seen until three post-natal months [72]. As in the cat
multisensory SC neurons, the newborn rhesus monkey also fails to integrate coincident cross-modal
inputs [74,75]. Thus, this capacity might indeed be strongly dependent on experiences [73,76].
Early post-natal experience is critical and deprivation of sensory information during this time can
lead to an inability to integrate signals neurologically [45,77]. Studies conducted on the effects of
sensory deprivation have demonstrated the significance of sensory organ stimulation to the proper
functioning and development of sensorineural structures. It is possible that MSI capacities increase in
precision over the course of human development and that they are progressively enriched through both
the maturation of brain systems and the accumulation of experience. Since newborns from all species
are first introduced with a complex and multisensorial environment, they ought to possess some neural
mechanisms allowing them to adapt to that environment promptly. Although these coping mechanisms
remain fragile and rudimentary, it is these mechanisms that allow their survival. This review exposes a
discrepancy in the data revealing that newborn animals cannot perform MSI at birth while there is
evidence that newborn humans can. This divergence may be accountable in the fact that animal
adaptation is specific to natural environments, and does not occur when the animal is viewing
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artificial stimuli such as gratings [78]. Nevertheless, the question whether MSI is innate or a product
of our environment remains debatable and requires further investigation.
2.2. Neuroanatomical Correlated of MSI and Pediatric Brain Activity
The recent explosion of EEGs and neuroimaging techniques has allowed the identification of
numerous multisensory convergence zones in the brain. Numerous cortical and subcortical brain
regions have been identified to receive afferent inputs from multiple senses. Subcortically, the SC and
the basal ganglia as well as association and other cortical regions including the superior temporal
sulcus, the parietal, premotor and prefrontal cortex [7982] are also implicated in MSI, including
feedback as well as feedforward anatomical projections [83,84]. Moreover, recent evidence at the
earliest stages of perceptual processing reveals multisensory modulations, activations and connectivity
in sensory sensory-specific brain areas [85,86].
To date, knowledge of the development of the neurophysiological processes that underlie MSI
comes largely from animal and adult studies. To our knowledge, one recent study using
electrophysiology (ERP) [87] has investigated the development of MSI capacities in infants. In this
study, Reynolds and colleagues (2014) [87] have shown evidence of enhance neural responsiveness to
synchronous audiovisual stimulation compared to asynchronous stimulation in five-month-old infants.
Besides, only a few studies have dealt with the underlying cerebral mechanisms of MSI in older
children and teenagers. It is in particular the case of Brandwein, Foxe, Russo, Altschuler, Gomes and
Molholm (2011) [88] who used ERP to characterize the developmental trajectory of brain processes
underlying audiovisual MSI in forty-nine neurotypical children and adolescents aged between 7- and
16-years-old. The data suggest that mature levels of multisensory facilitation are only reached by
approximately 15 years of age. Another ERP study in typically developing children aged between
6- and 13-years-old suggests that like adults, they integrate multisensory audio-somatosensory input
during multiple stages of sensory information processing [89]. However, a study in
magnetoencephalography revealed a robust audio-somatosensory integration response in 11- and
13-month-old infants, which suggest the development of MSI during the first year of life [90].
As outlined above, these studies provide encouraging evidence for cortical MSI in typical children.
However, considering the important discrepancy in neurophysiological data, further exploration of
MSI in neurotypical children is required. The use of neuroimaging approach is of great interest for the
scientific community and could fill the current gap of knowledge on developmental MSI.
3. MSI and Cognitive Development
As previously stated, multisensory stimuli provide an enhanced representation of the environment [91]
and MSI processes facilitate the speed and accuracy of a variety of behaviors and perceptual processes.
The benefits of multisensory information derive from empirical support with infants in various
domains showing that multisensory stimulation can enhance early perceptual, affective, and cognitive
discrimination. For instance, the combined use of information from several senses has been found to
enhance time discrimination abilities in infants [16,33] as well as affect discrimination [41] and even
numerical cognition in infants [92,93] and preschool children [94]. Multisensory stimulation promotes
heightened attention, perceptual processing and memory in adults as well as in infants [16,95]. Some
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authors have put forward that the capacity to perceive a complete and coherent representation of multimodal
information provides the groundwork for the development of perception, cognition and behavioral abilities,
which, in turn, are critical elements to the development of higher-level perceptual and cognitive
functions [96,97]. The acquisition of MSI capacity would influence perceptual learning [16] and the
acquisition of global cognitive and intellectual abilities [98,99]. Therefore, these MSI capacities in infancy
may provide an important developmental foundation for the emergence of cognitive abilities in adulthood.
The premise that MSI can contribute to cognitive development has been supported by studies
showing lower intellectual functioning in children with MSI deficits [99101]. Some studies showed
that information transfer across different modalities predict verbal performance in school age children,
suggesting that primary MSI skills can impact the acquisition of verbal aptitudes [99,100]. For instance,
recent findings showed that children who did not demonstrate good MSI skills had weaker verbal
processing scores than what was expected when considering their age and global intellectual
quotient [101]. Moreover, sensory integration deficits might result in various difficulties such as learning
new skills, getting organized, regulating attention and engaging in positive social experiences in some
children [102]. These kinds of difficulties in integrating multisensory information might be associated
with particular neurodevelopmental disorders in children.
4. MSI in Neurodevelopmental Disorders
According to the World Health Organization, neurodevelopmental disorders affect one in six
children in industrialized countries [103]. Impacting cerebral growth and development,
neurodevelopmental disorders encompass a wide range of disorders, such as intellectual disability,
Tourette syndrome, autism spectrum disorder, learning disabilities and attention deficit disorder with
or without hyperactivity (ADD/ADHD). Children with neurodevelopmental disorders also represent a
significant proportion of students who are struggling or failing in school [104,105]. A better
understanding of these disorders thus appears to be a crucial concern, particularly when embracing a
therapeutic and preventive perspective. Therefore, the following sections will examine the relationship
between MSI deficits and two neurodevelopmental disorders commonly found in children:
Developmental dyslexia [106] and attention deficit disorder with or without hyperactivity (ADD/ADHD).
4.1. MSI and Dyslexia
Developmental dyslexia is a specific reading and spelling deficit affecting 4% to 10% of the
population [107]. According to the Fifth Edition of the Diagnostic and Statistical Manual of Mental
Disorders (DSM-V) [106], this neurodevelopmental disorder manifests itself during the years of formal
schooling and is characterized by persistent and impairing difficulties with learning foundational
academic skills in reading, such as reading fluently with an accurate comprehension, despite average
or above-average intelligence [106,108].
Deficits in the phonological domain have consistently been found to be the primary cause of
developmental dyslexia [109112], although other cognitive deficits, such as in working
memory [113,114], executive functions [115118], processing speed [119121] and attention [122]
have been linked to this disorder. Although a number of conceptual frameworks have been put forward
to explain the spectrum of neurological deficits seen in dyslexia, we will review the phonological-deficit
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hypothesis and the temporal processing hypothesis, two models of particular interest for
developmental MSI.
4.1.1. MSI and the Phonological-Deficit and Temporal Processing Hypothesis
The phonological-deficit hypothesis supposes that reading and spelling difficulties result from
impaired phonological processes specific to language [107,123,124]. MSI is undoubtedly an important
competence in the acquisition of reading skills, since they rely upon rapid and accurate associations
between the visual (written) and auditory (verbal) labels [125127]. Regardless of phonological
awareness difficulties, authors have suggested that children with dyslexia have difficulties associating
verbal labels to the appropriate visual stimuli and thus, establishing appropriate associations between a
word and its spelling [127,128]. A number of studies have put forward that unstable letter-speech sound
associations could be a critical factor in dyslexia [129,130]. It has been found that children with
developmental dyslexia showed significant deficits in processing letter and digit strings (verbal
material) [131]. These results receive strong support from a neuroimaging study by Blau and
colleagues (2010) [132] showing fundamental deficits in letter-sound integration in children with
dyslexia. Similarly, recent findings on the influence of processing speed on reading acquisition in
six-year-old children revealed that, whatever the modality (audio-verbal, visuo-verbal, visual, and
visuo-visual), children with reading difficulties displayed poor performances in rapid intermodal
processing speed in audio-verbal (phonological awareness) and visuo-verbal (rapid naming) tasks [133].
These results support the influence of MSI in rapid naming and phonological processes involved in
reading, suggesting that the neural mechanisms underlying audio-visual integration in children with
dyslexia differ from normal reading children.
Other studies postulated that not only unimodal [125,134,135] but also multisensory verbal and
nonverbal information processing is temporally impaired in children with dyslexia. Some evidence
suggests that the core deficit of dyslexia is based on atypical temporal processing of audio-visual
multisensory information [125,135138]. An interesting paradigm to investigate intermodal temporal
processing is the McGurk effect [139]. This effect occurs when an individual sees and hears a speaker
producing speech segments that are incongruent with their visual perception. For instance, a classic
McGurk effect is hearing the syllable /ta/ while the speaker uttered /ga/. Thus, the auditor usually
perceives the sound /pa/. This robust effect in neurotypical individuals was found to be impaired in
subjects with dyslexia, suggesting a deficit of MSI. For that matter, instead of perceiving the normal
illusion, individuals with dyslexia tend to pronounce the sound perceived visually [140].
Similarly, children with reading difficulties showed low performances in comparing two patterns of brief
nonverbal audio-visual stimuli [141]. Moreover, decreased segregation acuity and prolonged cross-modal
segregation times were also evident using trains of brief stimuli in three different sensory modalities
(audio-visual, audio-tactile and visuo-tactile) in 8- to 12-year-old children with dyslexia, especially in
the audio-visual condition [142]. These findings suggest the implication of a general impairment of the
nervous system in children with dyslexia when processing audio-visual information rather than a sole
deficit in the sensory, motor or phonological systems.
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with visual letters (congruent or incongruent) also showed reduced neural integration in the left
planum temporale and Heschl sulcus and the left superior temporal sulcus [132]. Overall, these studies
suggest that an interrelated network of visual, auditory and heteromodal brain areas might contribute to
the skilled use of letter-speech sound integration necessary for learning to read. Reduced congruency
between letters and speech sounds in children with dyslexia are likely to indicate less successful
letter-speech sound integration [132]. The presence of deviant patterns of activation and morphological
brain alterations associated with MSI may play a critical role in the neural basis of dyslexia. Despite
the gap of knowledge on this matter, these results highlight the importance of pursuing such neuroimaging
studies in order to better understand the impact of MSI deficits on children with reading disabilities.
Atypical development of MSI capacities during infancy can have a momentous impact on childrens
neurodevelopment. The previous findings suggest that children with dyslexia have difficulties in MSI
and may suffer from integrating sensory cues coming from multiple sources. The hypothesis that MSI
deficits might be responsible for impaired reading is still premature. The impact of such difficulties
remains unclear and requires greater attention from researchers. However, the development of this
integrative ability may offer a cue that may be useful in identifying children likely to develop later
difficulties. Therefore, we can speculate that children with dyslexia would take advantage of intervention
protocols directed to improve sensory integration.
4.2. MSI and Attention Deficit Disorder with or without Hyperactivity (ADD/ADHD)
ADHD occurs in most cultures in about 3% to 5% of children [107,160] and accounts for
approximately half of all pediatric referrals to mental health services in the United States [161,162].
ADD/ADHD is a neurodevelopmental disorder characterized by impairing levels of inattention,
disorganization, and/or hyperactivity-impulsivity that interferes with functioning or development.
Inattention and disorganization entail inability to stay on task, to give close attention to details, to
listen when spoken to, to follow through on instructions, to be easily distracted by extraneous stimuli
and to have difficulty organizing tasks and activities, at levels that are inconsistent with age or
developmental level [107]. Hyperactivity refers to excessive motor activity when it is not appropriate
or excessive fidgeting or tapping hands or feet when seated, difficulty to remain seated in situations
where it is expected, overactivity, talking excessively, at levels that are inconsistent with age or
developmental level [107]. Impulsivity implies a desire for immediate rewards or an inability to delay
gratification which can manifest into behaviors such as a difficulty to wait for her/his turn, interrupting
or intruding into other peoples activities and making important decisions without consideration of
long-term consequences, at levels that are inconsistent with age or developmental level [107].
According to the DSM-V, ADHD symptoms must be present in at least two settings, impact directly on
social and academic activities and must be present before the age of 12-years-old [107]. While the
predominantly inattentive type (ADHD-I) is the most common subtype in the population (38%57% of
all individuals with ADHD), individuals with the combined inattention-hyperactivity type (ADHD-C)
(22%26%) are more likely to be referred for clinical services [163].
Additionally to attention problems, ADHD is often accompanied by deficits other than those
subsumed under the ADHD diagnosis. In terms of cognitive profile, children with ADHD often have
difficulty with executive functions (e.g., planning, set shifting, organization, inhibition and regulation
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of behavior) as well as processing speed and working memory [164176]. A high percentage of
children with attention disorders also have sensory processing problems, exemplified by behavioral
evidence of difficulty modulating sensory responses [177179]. It has been reported that boys with
ADHD aged between 6- and 10-year-old have more sensory processing difficulties than neurotypical
boys [180]. It has also been suggested that these children may not be perceiving and processing
sensory information properly as well as having difficulty producing appropriate responses at school, at
home and in the community [181]. Compared with children without neurodevelopmental disorders,
children with ADHD exhibit greater difficulties in the sensorimotor domain such as the vestibular and
balance control systems [182,183]. For instance, in contrast to neurotypical children, Hassan and Azzam
(2012) [184] showed that children with ADHD-C aged between 8- and 10-year-old had lower
somatosensory, visual and vestibular ratios by 1%, 9%, and 18%, respectively. According to
Guskiewicz and Perrin (1996) [185], this could be the result of a lack of adequate interaction among
the three sensory inputs that provide orientation information to the postural control system.
Furthermore, children with ADHD also have more difficulties to process tactile [186], visual [187] and
auditory stimuli [188191]. More precisely, while Hern and Hynd (1992) [186] found that 6- and
12-year-old children with ADHD-C exhibit more soft signs than the normal group on a prototype
sensorimotor soft sign battery. Ghanizadeh (2010) [187] demonstrated that children with ADHD give
poorer performances on visual acuity and visual field. In the audition realm, a number of studies
reported auditory processing problems in children with ADHD [188191].
4.3. Neuroanatomical Model for ADHD
Studies investigating the neural basis of ADHD have steadily showed structural and/or functional
anomalies in cortical areas, basal ganglia, and cerebellar brain regions in children with ADHD [192194].
This circuit has been extensively investigated using methods such as structural volumetric brain
imaging and fMRI and has been linked to ADHD behavioral deficits such as inhibitory response,
working memory and executive functioning impairments [194203]. For instance, using volumetric brain
imaging to examine anatomic brain abnormalities, an extensive study compared regional brain volumes in
152 children and adolescents with ADHD aged 5 to 18 years old and 139 age- and sex-matched
controls [204]. Children with ADHD exhibited smaller total cerebral and cerebellar volumes in
contrast to control children and these volumetric differences persisted into adulthood. Furthermore,
frontal and temporal gray matter, caudate nucleus and cerebellar volumes correlated with the severity
of ADHD symptoms [204]. Other studies investigating volumetric differences between children with
ADHD and typically developing children also reported smaller cerebral volume in frontal and
prefrontal cortices [205207]. Such cortical volume reductions were also associated with altered brain
activation in sensory cortices (auditory, visual and somatosensory cortices) [184,208], which could
explain sensorimotor deficits in this population. The frontal lobes both receive a multitude of inputs
from sensory association areas and have influence over a wide region of the nervous system to direct
behavior. Moreover, working memory, planning, and reasoning, often affected in ADHD, are
associated to the frontal lobes and depend on the recognition and integration of a vast network of signals.
Research evidence in favor of the existence of bidirectional influences between attention and MSI is
thus considerable and allows the possibility to make neuroanatomical connections between ADHD and
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MSI networks. Attentional processes and MSI share subcortical networks such as the SC [209] and
operate with cortical regions, including the fronto-parietal and temporo-parietal networks [210].
Moreover, top-down attention is controlled by a fronto-parietal network of brain areas, which sends
signals that modulate the sensitivity of neurons in sensory brain regions [211]. Recently, Koziol et al.
(2011,2012) [192,212] integrated SPD/SMD symptoms in relation to their impacts upon the
development of inhibitory control, working memory, academic skill, and behavioral automation in
children with ADHD, proposing the first neuroanatomical conceptualization model of sensory
processing deficits in ADHD. They suggested that an integrative network of specific brain regions is
involved in both cognitive development and sensorimotor integration of the environment [212,213].
According to their model, the cortex encodes specific sensory information (visual, auditory, spatial,
perceptual and sensory) by interacting with the basal ganglia that act as a selection mechanism and is
important to voluntary motor movement, perceptual learning and inhibitory response. Then, the
cerebellum receives sensory information inputs from the involved cortical regions and basal ganglia in
order to integrate stimuli and modulate or regulate the intensity of experienced stimulation [212,213].
As previously mentioned, similarly to the neurons in the SC and related structures, previous studies
have demonstrated the presence of multisensory neurons in the basal ganglia [85]. Neurons sensitive to
visual, auditory or somatosensory modalities have been found in both the substantia nigra (SN) and the
caudate nucleus (CN) in which a high proportions of neurons with multisensory properties have been
described in these neuronal populations [214,215]. MSI deficits in the CN and the SN may lead to a
disruption in the processing of complex sensory stimuli which, indirectly will affect the sensory
feedback of motor actions controlled by the basal ganglia. Studies have documented anatomical
abnormalities, such as volume decrease, asymmetric and connectivity differences, in the basal
ganglia [203,208] and cerebellum of children with ADHD [203,216219].
Overall, the neural basis of ADHD has been widely documented by functional and structural studies.
Anatomical evidence has provided a reasonable framework for the suggestion that ineffective MSI
cortical maps underlying sensory-related behaviors as well as physiological reactivity to sensory stimuli
found in children with both ADHD and sensory processing problems may possibly explain
their comorbidity.
5. Conclusions
One of the most impressive features of the central nervous system is its ability to process
information from a variety of stimuli to produce an integrated, comprehensive representation of the
external world. Research in neurotypical adults has repeatedly shown behavioral benefits of MSI that
might be linked to the underlying ability of the brain to integrate different sensory inputs related to a
single event [11]. The benefits of the combined use of information from several senses have been
exposed in numerous studies and reveal notably that MSI aids detection and speed response [29].
Although MSI capacity has been extensively studied in adults, the literature is scarcer regarding the
ability to integrate multisensory information in infants. This review firstly aimed to describe MSI
developmental processes of neurotypical infants and children and its neuroanatomic correlates.
Moreover, we addressed the question whether the capacity to integrate multisensory information exist
from birth or develops as a result of experience. The debate between MSI being innate or acquired
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remains. Neurophysiological data on animals [59,60,63] and ERP studies on children and
adolescents [65,66] suggest that our optimal capacity to integrate multisensory information reaches its
maturity late during childhood and is strongly dependent on early experience.
The second section of this article reviewed the presence of sensory integration impairments in
children affected with a neurodevelopmental disorder. We first studied dyslexia and paid a particular
attention to the phonological-deficit and the temporal processing hypothesis, two models of special
interest for developmental MSI. Overall, the literature suggests that an interrelated network of visual,
auditory and heteromodal brain areas contributing to the skilled use of letter-speech sound integration
might be impaired in children with dyslexia. Studies on ADHD also reported potential alterations of
MSI. Children with ADHD often show sensory deficits including sensorimotor [166,167],
somatosensory [168], visual [171] and auditory [172175] processing impairments. Moreover, anatomical
evidence suggested that ineffective MSI cortical maps underlying sensory-related behaviors as well as
physiological reactivity to sensory stimuli found in both children with ADHD and sensory processing
problems may possibly explain their comorbidity. Although certain neurodevelopmental disorders can
cause MSI impairments, research and clinical applications in development are in progress and constitute
promising research avenues.
Acknowledgments
This work was funded by scholarships granted by the Fonds de la Recherche du Qubec-Sant, the
Fonds de recherche du QubecNature et technologies (Emmanuelle Dionne-Dostie), the Fondation
des toiles, CHU Ste-Justine Research Center (Emmanuelle Dionne-Dostie, Natacha Paquette) and the
Canadian Institute of Health Research (Natacha Paquette). It was also supported by the Canada
Research Chair program held by Maryse Lassonde and grants from the Canadian Institutes of Health
Research and the Fonds de la Recherche du Qubec Sant held by Anne Gallagher and Maryse Lassonde.
Author Contributions
All authors have been involved in the preparation and have approved the submitted manuscript.
Emmanuelle Dionne-Dostie was lead author and responsible for conducting the literature review and
writing the manuscript. Natacha Paquette participated in the redaction of the MSI and
neurodevelopmental disorders section. Maryse Lassonde reviewed and edited the manuscript. As the
senior author, Anne Gallagher supervised Emmanuelle Dionne-Dostie and Natacha Paquettes work,
reviewed and edited the manuscript.
Conflicts of Interest
The authors declare no conflict of interest.
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